[go: up one dir, main page]

AR067850A1 - METHODS AND COMPOSITIONS TO INHIBIT THE EDEMA FACTOR AND ADENILIL CYCLASE AND KIT - Google Patents

METHODS AND COMPOSITIONS TO INHIBIT THE EDEMA FACTOR AND ADENILIL CYCLASE AND KIT

Info

Publication number
AR067850A1
AR067850A1 ARP080102569A ARP080102569A AR067850A1 AR 067850 A1 AR067850 A1 AR 067850A1 AR P080102569 A ARP080102569 A AR P080102569A AR P080102569 A ARP080102569 A AR P080102569A AR 067850 A1 AR067850 A1 AR 067850A1
Authority
AR
Argentina
Prior art keywords
group
substituted
pyridyl
alkyl
unsubstituted
Prior art date
Application number
ARP080102569A
Other languages
Spanish (es)
Inventor
Mary Ann Walter
Scott R Gilbertson
Maria Estrella-Jimenez
Jian Gao
Johnny W Peterson
Catherine H Schein
Deliang Chen
Original Assignee
Mission Pharma Co
Univ Texas
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=40468705&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=AR067850(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Mission Pharma Co, Univ Texas filed Critical Mission Pharma Co
Publication of AR067850A1 publication Critical patent/AR067850A1/en

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/12Ketones
    • A61K31/122Ketones having the oxygen directly attached to a ring, e.g. quinones, vitamin K1, anthralin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/185Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
    • A61K31/19Carboxylic acids, e.g. valproic acid
    • A61K31/192Carboxylic acids, e.g. valproic acid having aromatic groups, e.g. sulindac, 2-aryl-propionic acids, ethacrynic acid 
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/21Esters, e.g. nitroglycerine, selenocyanates
    • A61K31/215Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
    • A61K31/216Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acids having aromatic rings, e.g. benactizyne, clofibrate
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/335Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/34Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/47Quinolines; Isoquinolines
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/12Antidiarrhoeals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00Drugs for genital or sexual disorders; Contraceptives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04Antibacterial agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

Landscapes

  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Communicable Diseases (AREA)
  • Emergency Medicine (AREA)
  • Oncology (AREA)
  • Rheumatology (AREA)
  • Pain & Pain Management (AREA)
  • Endocrinology (AREA)
  • Reproductive Health (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

Se describen un método para tratar y/o prevenir la pérdida de fluido intestinal en un sujeto que comprende administrarle al sujeto una composicion que comprende una cantidad eficaz para el uso terapéutico de un compuesto o una sal de éste aceptable para el uso farmacéutico, donde la formula general del compuesto se selecciona del grupo que consiste en el grupo de formulas (1) a (9) y cualquier combinacion de éstas, donde 1) R es una estructura de anillo cíclico o bicíclico; 2) R1 es un hidrogeno, una estructura de anillo cíclico o bicíclico; 3) R2 es un hidrogeno, alquilo, una estructura de anillo cíclico o bicíclico; 4) R3 es un hidrogeno, o alquilo; 5) R5 es un hidrogeno, alquilo, una estructura de anillo cíclico o bicíclico; 6) X es un alquilo, oxígeno, un éster, una amina o una amida, 7) Z se selecciona del grupo que consiste en hidrogeno, alquenilo, alquinilo, fenilo, bencilo, halo, fluoro, cloro, bromo, iodo, hidroxilo, ceto, oxo, aldo. carbonato, carboxilo, alcoxilo, éster, carboxamido, amino, amonio, imino, imido, azido, azo, cianato, isociano, isocianato, isotiocianato, nitroxilo, ciano, nitrosooxilo, nitro, nitroso, 4-piridilo, 3-piridilo, 2-piridilo, tioéter, sulfanilo, sulfo, sulfinilo, mercapto, sulfanilo, sulfhidrilo, sulfonamino, tiocianato, alquil amino, ácido hidroxiámico, metilo, etilo, 1,3-dioxilanilo, propilo, iso-propilo, butilo, ter-butilo, alquilo no sustituido o sustituido, ramificado o no ramificado, alquenilo C1-3, arilo no sustituido o sustituido, ramificado o no ramificado, alquilarilo no sustituido o sustituido, ramificado o no ramificado, hidrato de carbono no sustituido a sustituido, ramificado o no ramificado; 8) W se selecciona de! grupo que consiste en CO, NH, metileno, un átomo de azufre, un átomo de oxigeno y tionilo; y 9) n es 0, 1,o más de 1. También se describen composiciones que comprenden compuestos de formula 1 y 4 y un kit o conjunto de elementos para el tratamiento de la pérdida de fluido intestinal en un sujeto, que comprende una cantidad terapéuticamente efectiva de un compuesto a una sal farmacéuticamente aceptable del mismo de formula general seleccionada del grupo que consiste de las formulas 1 a 9. Reivindicacion 2: El método de la reivindicacion 1, donde R está sustituido o no sustituido, y se selecciona del grupo que consiste en fenilo, piranonilo, piridilo, imidazolilo, 1,8-naftiridinilo y N-oxido de piridilo. Reivindicacion 4: El método de la reivindicacion 1, donde R1 esté sustituido o no sustituido, y se selecciona del grupo que consiste en fenilo, piridilo y furanilo. Reivindicacion 14: El método de la reivindicacion 1, donde la composicion se administra en combinacion con una o más drogas adicionales. Reivindicacion 15: El método de la reivindicacion 1, donde la composicion comprende además un antibiotico o un antiinflamatorio. Reivindicacion 78: El conjunto de elementos de la reivindicacion 70, que comprende además una droga seleccionada del grupo que consiste en un antibiotico, un antidiarreico y una droga inhibidora de LT.A method for treating and / or preventing the loss of intestinal fluid in a subject comprising administering to the subject a composition comprising an amount effective for the therapeutic use of a compound or a salt thereof acceptable for pharmaceutical use, wherein General formula of the compound is selected from the group consisting of the group of formulas (1) to (9) and any combination thereof, where 1) R is a cyclic or bicyclic ring structure; 2) R1 is a hydrogen, a cyclic or bicyclic ring structure; 3) R2 is a hydrogen, alkyl, a cyclic or bicyclic ring structure; 4) R3 is a hydrogen, or alkyl; 5) R5 is a hydrogen, alkyl, a cyclic or bicyclic ring structure; 6) X is an alkyl, oxygen, an ester, an amine or an amide, 7) Z is selected from the group consisting of hydrogen, alkenyl, alkynyl, phenyl, benzyl, halo, fluoro, chloro, bromo, iodo, hydroxyl, keto, oxo, aldo. carbonate, carboxyl, alkoxy, ester, carboxamido, amino, ammonium, imino, imido, azido, azo, cyanate, isocyanate, isocyanate, isothiocyanate, nitroxyl, cyano, nitrosooxyl, nitro, nitroso, 4-pyridyl, 3-pyridyl, 2- pyridyl, thioether, sulfanyl, sulfo, sulfinyl, mercapto, sulfanyl, sulfhydryl, sulfonamino, thiocyanate, alkyl amino, hydroxyamic acid, methyl, ethyl, 1,3-dioxylanyl, propyl, iso-propyl, butyl, tert-butyl, non-alkyl substituted or substituted, branched or unbranched, C1-3 alkenyl, unsubstituted or substituted, branched or unbranched aryl, unsubstituted or substituted, branched or unbranched alkylaryl, unsubstituted to substituted, branched or unbranched carbohydrate; 8) W is selected from! group consisting of CO, NH, methylene, a sulfur atom, an oxygen atom and thionyl; and 9) n is 0, 1, or more than 1. Compositions comprising compounds of formula 1 and 4 and a kit or set of elements for the treatment of loss of intestinal fluid in a subject, comprising an amount, are also described. therapeutically effective of a compound to a pharmaceutically acceptable salt thereof of the general formula selected from the group consisting of formulas 1 to 9. Claim 2: The method of claim 1, wherein R is substituted or unsubstituted, and is selected from the group consisting of phenyl, pyranonyl, pyridyl, imidazolyl, 1,8-naphthyridinyl and pyridyl N-oxide. Claim 4: The method of claim 1, wherein R1 is substituted or unsubstituted, and is selected from the group consisting of phenyl, pyridyl and furanyl. Claim 14: The method of claim 1, wherein the composition is administered in combination with one or more additional drugs. Claim 15: The method of claim 1, wherein the composition further comprises an antibiotic or an anti-inflammatory. Claim 78: The set of elements of claim 70, further comprising a drug selected from the group consisting of an antibiotic, an antidiarrheal and an LT inhibitor drug.

ARP080102569A 2007-06-15 2008-06-17 METHODS AND COMPOSITIONS TO INHIBIT THE EDEMA FACTOR AND ADENILIL CYCLASE AND KIT AR067850A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US94437507P 2007-06-15 2007-06-15
US3526908P 2008-03-10 2008-03-10

Publications (1)

Publication Number Publication Date
AR067850A1 true AR067850A1 (en) 2009-10-28

Family

ID=40468705

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP080102569A AR067850A1 (en) 2007-06-15 2008-06-17 METHODS AND COMPOSITIONS TO INHIBIT THE EDEMA FACTOR AND ADENILIL CYCLASE AND KIT

Country Status (12)

Country Link
US (2) US8003692B2 (en)
EP (1) EP2166841A4 (en)
CN (1) CN101784274A (en)
AR (1) AR067850A1 (en)
AU (1) AU2008302667B2 (en)
BR (1) BRPI0813176A2 (en)
CA (1) CA2692004C (en)
CL (1) CL2008001782A1 (en)
CO (1) CO6270184A2 (en)
DO (1) DOP2009000272A (en)
MX (1) MX2009013676A (en)
WO (1) WO2009038842A2 (en)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008121171A1 (en) * 2007-01-12 2008-10-09 Cornell Research Foundation, Inc. Adenylyl cyclases as novel targets for antibacterial interventions
US9095578B2 (en) * 2007-01-12 2015-08-04 Cornell Research Foundation, Inc. Adenylyl cyclases as novel targets for the treatment of infection by eukaryotic pathogens
AU2008302667B2 (en) * 2007-06-15 2014-07-10 Board Of Regents, The University Of Texas System Methods and compositions to inhibit edema factor and adenylyl cyclase
CN102159948B (en) * 2008-07-22 2014-06-25 普罗美加公司 Luminescent Phosphotransferase or ATP Hydrolase Assay Based on ADP Detection
JP5730190B2 (en) * 2009-03-31 2015-06-03 株式会社レナサイエンス Plasminogen activator inhibitor-1 inhibitor
AU2013207510A1 (en) 2012-01-06 2014-07-31 The Regents Of The University Of California Compositions, methods of use, and methods of treatment
US10092537B2 (en) 2013-04-15 2018-10-09 Renascience Co., Ltd. Use for PAI-1 inhibitor
JP6510041B2 (en) 2014-10-08 2019-05-08 プロメガ コーポレイションPromega Corporation Bioluminescent succinate detection assay
CN105218343B (en) * 2015-10-26 2017-03-22 乐普药业股份有限公司 Synthesis method of 3-bromocyclohex-2-enone
US10556853B2 (en) * 2017-01-10 2020-02-11 Owen-Barry Pharmaceuticals Inc. Anticonvulsant compounds
IL273428B2 (en) 2017-09-22 2023-09-01 Jubilant Epipad LLC Heterocyclic compounds as pad inhibitors
US10882821B1 (en) 2017-09-26 2021-01-05 The Board Of Trustees Of The Leland Stanford Junior University Enantiomeric compound for the reduction of the deleterious activity of extended nucleotide repeat containing genes
CN111225915B (en) 2017-10-18 2023-03-07 朱比兰特埃皮帕德有限公司 Imidazopyridine compounds as PAD inhibitors
BR112020008851A2 (en) 2017-11-06 2020-10-20 Jubilant Prodel LLC compound of formula i, process for preparing compounds of formula i, pharmaceutical composition, method for treating and / or preventing various diseases, use, method for treating cancer, method of treating cancer and method for treating and / or prevention of cancer and infectious diseases
JP7368369B2 (en) 2017-11-24 2023-10-24 ジュビラント・エピスクライブ・エルエルシー Heterocyclic compounds as PRMT5 inhibitors
JP7279063B6 (en) 2018-03-13 2024-02-15 ジュビラント プローデル エルエルシー Bicyclic compounds as inhibitors of PD1/PD-L1 interaction/activation

Family Cites Families (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4066834A (en) 1974-01-24 1978-01-03 Miles Laboratories, Inc. Cycloalkenyl analogues of prostaglandins E
US4222944A (en) 1978-07-31 1980-09-16 Hoffmann-La Roche Inc. Halo-3-dibenzofuran alkanonitriles
KR20000068415A (en) 1996-09-04 2000-11-25 로즈 암스트롱, 크리스틴 에이. 트러트웨인 Compounds for and a Method of Inhibiting Matrix Metalloproteinase
CA2366877A1 (en) 1999-03-22 2000-09-28 Stanley Michael Roberts Chemical compounds and their uses
MXPA02012002A (en) * 2000-06-08 2004-09-06 Univ Texas Heterocycle derivatives and methods of use.
AU2002239277A1 (en) * 2000-11-20 2002-05-27 Cor Therapeutics, Inc. Adenine based inhibitors of adenylyl cyclase, pharmaceutical compositions and method of use thereof
AU2002217316A1 (en) * 2001-01-03 2002-07-30 Medpharma Plc Use of terpenes for the treatment of digestive tract infections
DE10123163A1 (en) * 2001-05-09 2003-01-16 Gruenenthal Gmbh Substituted cyclohexane-1,4-diamine derivatives
EP1431267A4 (en) * 2001-08-09 2004-12-22 Ono Pharmaceutical Co Carboxylic acid derivative compounds and drugs comprising these compounds as the active ingredient
AU2002352402A1 (en) * 2001-12-14 2003-06-30 Charterhouse Therapeutics Limited Improvements in pharmaceutical compositions
US20030157159A1 (en) * 2002-01-15 2003-08-21 Franklin Lanny Udell Prevention and treatment of digestive tract infections
US20030224403A1 (en) 2002-02-27 2003-12-04 Popov Serguei G. Lethal toxin cytopathogenicity and novel approaches to anthrax treatment
RU2293721C2 (en) * 2002-02-28 2007-02-20 Джапан Тобакко Инк. Ester compounds and their using in medicine
DE60317918T2 (en) * 2002-10-23 2009-01-29 Glenmark Pharmaceuticals Ltd. TRICYCLIC COMPOUNDS FOR THE TREATMENT OF INFLAMMATORY AND ALLERGIC DISEASES METHOD OF PREPARING THEM AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEY
WO2005005415A1 (en) * 2003-07-09 2005-01-20 Biolipox Ab Indoles useful in the treatment of inflammation
WO2005028467A1 (en) * 2003-09-15 2005-03-31 Anadys Pharmaceuticals, Inc. Antibacterial 3,5-diaminopiperidine-substitute aromatic and heteroaromatic compounds
NZ587549A (en) * 2004-06-24 2012-10-26 Vertex Pharma 6-Amino-indole derivatives and processes for their preparation
WO2006039356A2 (en) * 2004-09-29 2006-04-13 Cytovia, Inc. Substituted n-aryl-9-oxo-9h-fluorene-1-carboxamides and analogs as activators of caspases and inducers of apoptosis
US7091231B2 (en) 2004-12-10 2006-08-15 Allergan, Inc. 12-Aryl prostaglandin analogs
WO2007076055A2 (en) * 2005-12-22 2007-07-05 Entremed, Inc. Compositions and methods comprising proteinase activated receptor antagonists
EP2029594B1 (en) * 2006-05-23 2010-10-20 NeuroSearch A/S Novel 1,4-diaza-bicyclo[3.2.2]nonane derivatives and their medical use
AU2008302667B2 (en) * 2007-06-15 2014-07-10 Board Of Regents, The University Of Texas System Methods and compositions to inhibit edema factor and adenylyl cyclase

Also Published As

Publication number Publication date
AU2008302667A1 (en) 2009-03-26
US8003692B2 (en) 2011-08-23
CA2692004A1 (en) 2009-03-26
DOP2009000272A (en) 2010-02-15
WO2009038842A3 (en) 2009-12-30
CA2692004C (en) 2013-04-09
EP2166841A4 (en) 2014-05-07
US20120010233A1 (en) 2012-01-12
CN101784274A (en) 2010-07-21
MX2009013676A (en) 2010-06-01
AU2008302667B2 (en) 2014-07-10
BRPI0813176A2 (en) 2014-12-30
US20090093519A1 (en) 2009-04-09
EP2166841A2 (en) 2010-03-31
WO2009038842A2 (en) 2009-03-26
CL2008001782A1 (en) 2008-11-03
CO6270184A2 (en) 2011-04-20

Similar Documents

Publication Publication Date Title
AR067850A1 (en) METHODS AND COMPOSITIONS TO INHIBIT THE EDEMA FACTOR AND ADENILIL CYCLASE AND KIT
ES2345044T3 (en) 2-PIPERAZIN-PIRIDINES USEFUL TO TREAT THE PAIN.
NO20060972L (en) Pyridyl derivatives and their use as therapeutic agents
CA2412968A1 (en) Substituted pyridines as selective cyclooxygenase-2 inhibitors
RU2017138972A (en) Human Immunodeficiency Virus Replication Inhibitors
ES2300613T3 (en) THERAPEUTIC DERIVATIVES OF PIPERACINA USEFUL TO TREAT THE PAIN.
ES2309564T3 (en) PHENYL-CARBOXAMIDE COMPOUNDS USEFUL FOR THE TREATMENT OF PAIN.
CA2565813A1 (en) Substituted methyl aryl or heteroaryl amide compounds
RU2011108563A (en) THALASSEMIA TREATMENT METHODS
ES2317052T3 (en) USEFUL THERAPEUTIC AGENTS FOR THE TREATMENT OF PAIN.
WO2019204354A1 (en) Spirocyclic compounds
HRP20030450B1 (en) Isoindolin-1-one glucokinase activators
AR024732A1 (en) METHOD FOR THE TREATMENT OF CHRONIC PAIN THROUGH THE USE OF MEK INHIBITORS.
GB1114069A (en) Benzimidazole derivatives and anthelmintic compositions containing them
RU2010126105A (en) Pyridine derivatives substituted by a heterocyclic ring and a phosphonoxymethyl group and containing antifungal agents
KR910014350A (en) 3-aminopiperidine derivatives and related nitrogen-containing heterocyclic compounds
PE20090641A1 (en) HETERO CYCLIC AMIDES
ES2318045T3 (en) DERIVATIVES OF 1H-IMIDAZOL THAT HAVE AGONIST ACTIVITY CB1, PARTIAL AGONIST CB1 OR ANTAGONIST OF CB1.
HRP20080549T3 (en) 1,3,5-trisubstituted 4,5-dihydro-1h-pyrazole derivatives having cb1-antagonistic activity
CA2409741A1 (en) Tnf-.alpha. production inhibitors
WO2002064547A3 (en) Isophthalic acid derivatives as matrix metalloproteinase inhibitors
RU2011116227A (en) PYRAZOLOPYRIDINE DERIVATIVES AS NADPH-OXIDASE INHIBITORS
PT1487829E (en) Thiadiazolylpiperazine derivatives useful for treating or preventing pain
CA2437409A1 (en) Azoles as malonyl-coa decarboxylase inhibitors useful as metabolic modulators
ATE188467T1 (en) AMIDINO DERIVATIVES AS NO-SYNTHESIS INHIBITORS

Legal Events

Date Code Title Description
FB Suspension of granting procedure